RS Verma

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Zaslav A L; Fox J E; Jacob J; Kazi R; Allan S; Shklooskaya T; Sohal D; Kleyman S M; Verma R S
Significance of a prenatally diagnosed del(10)(q23).
Verma R S; Macera M J
Commentary: FISHing for the light at the ends of chromosomes.
Macera M J; Godec C J; Sharma N; Verma R S
Loss of heterozygosity of the TP53 tumor suppressor gene and detection of point mutations by the non-isotopic RNAse cleavage assay in prostate cancer.

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2002: Zaslav A L; Fox J E; Jacob J; Kazi R; Allan S; Shklooskaya T; Sohal D; Kleyman S M; Verma R S
Significance of a prenatally diagnosed del(10)(q23).
American journal of medical genetics 2002;107(2):174-6.
1999: Verma R S; Macera M J
Commentary: FISHing for the light at the ends of chromosomes.
European journal of human genetics : EJHG 1999;7(4):515-7.
1999: Macera M J; Godec C J; Sharma N; Verma R S
Loss of heterozygosity of the TP53 tumor suppressor gene and detection of point mutations by the non-isotopic RNAse cleavage assay in prostate cancer.
Cancer genetics and cytogenetics 1999;108(1):42-7.
1999: Conte R A; Samonte R V; Verma R S
Localization of subtelomeric sequences of human chromosomes 1q, 11p, 13q, and 16q in the higher primates.
Genetica 1999;105(1):31-4.
1999: Verma R S; Manikal M; Conte R A; Godec C J
Chromosomal basis of adenocarcinoma of the prostate.
Cancer investigation 1999;17(6):441-7.
1999: Azar G M; Conte R A; Kleyman S M; Logush A Z; Verma R S
Probing the human genome in search for a new 3q syndrome.
Annales de génétique 1999;42(2):95-100.
1999: Samonte R V; Conte R A; Verma R S
Localization of human midisatellite and macrosatellite DNA sequences on chromosomes 1 and X in the great apes.
Journal of human genetics 1999;44(1):57-9.
1998: Gogineni S K; Verma R S
An abortus with double trisomy (48,XY,+4,+7)
American journal of obstetrics and gynecology 1998;179(6 Pt 1):1654.
1998: Conte R A; Samonte R V; Verma R S
Evolutionary divergence of the oncogenes GLI, HST and INT2.
Heredity 1998;81 ( Pt 1)():10-3.
1998: Tarazami S T; Kringstein A M; Conte R A; Verma R S
Comparative mapping of the cri du chat and DiGeorge syndrome regions in the great apes.
Genes & genetic systems 1998;73(2):135-6.
1998: Macera M J; Smith L J; Frankel E; Szabo P; Verma R S
A Philadelphia negative chronic myelogenous leukemia with the chimeric BCR/ABL gene on chromosome 9 and a b3-a2 splice junction.
Cancer genetics and cytogenetics 1998;101(2):143-7.
1998: Verma R S; Ishwar L; Gogineni S K; Kleyman S M
Pericentromeric heteromorphism of human chromosome 18 as revealed by FISH-technique.
Annales de génétique 1998;41(3):154-6.
1998: Samonte R V; Conte R A; Verma R S
Molecular phylogenetics of the hominoid Y chromosome.
Journal of human genetics 1998;43(3):185-6.
1998: Verma R S; Kleyman S M; Conte R A
Chromosomal mosaicisms during prenatal diagnosis.
Gynecologic and obstetric investigation 1998;45(1):12-5.
1997: Ramesh K H; Qazi Q H; Verma R S
Direct insertion of euchromatic material from chromosome Y in the X-chromosome in hypogonadotropic hypogonadisms with Crohn's disease.
The Japanese journal of human genetics 1997;42(4):551-6.
1997: Verma R S; Kleyman S M; Conte R A
Variant euchromatic band within 16q12.1.
Clinical genetics 1997;52(6):446-7.
1997: Azar G M; DiPillo F; Gogineni S K; Godec C J; Verma R S
Highly complex chromosomal aberrations in bone marrow of a patient with metastatic prostate neoplasm.
Cancer genetics and cytogenetics 1997;99(2):116-20.
1997: Verma R S; Gogineni S K; Kleyman S M; Conte R A
Characterisation of a satellited non-fluorescent Y chromosome (Y[nfqs]) by FISH.
Journal of medical genetics 1997;34(10):817-8.
1997: Samonte R V; Conte R A; Verma R S
Brief communication: comparative mapping of the human estrogen receptor (ESR) and the Kallmann (KAL) regions to the chromosomes of the great apes.
American journal of physical anthropology 1997;103(4):561-3.
1997: Samonte R V; Conte R A; Verma R S
Physical mapping of human 7q and 14q subtelomeric DNA sequences in the great apes.
DNA research : an international journal for rapid publication of reports on genes and genomes 1997;4(3):249-52.
1997: Kumar C; Kleyman S M; Samonte R V; Verma R S
Marker chromosomes in fetal loss.
Human reproduction (Oxford, England) 1997;12(6):1321-4.
1997: Ramesh K H; Macera M J; Verma R S
Rapid denaturation improves chromosome morphology and permits multiple hybridizations during fluorescence in situ hybridization.
Biotechnic & histochemistry : official publication of the Biological Stain Commission 1997;72(3):141-3.
1997: Azar G M; Gogineni S K; Hyde P; Verma R S
Highly complex chromosomal abnormalities in plasma cell leukemia as detected by FISH technique.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(5):772-4.
1997: Gogineni S K; Shah H O; Chester M; Lin J H; Garrison M; Alidina A; Bayani E; Verma R S
Variant complex translocations involving chromosomes 1, 9, 9, 15 and 17 in acute promyelocytic leukemia without RAR alpha/PML gene fusion rearrangement.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(4):514-8.
1997: Conte R A; Kleyman S M; Kharode C; Verma R S
Delineation of a ring chromosome 16 by the FISH-technique: a case report with review.
Clinical genetics 1997;51(3):196-9.
1997: Platica M; Verma R S; Macera M J; Platica O
LNCaP-OM, a new androgen-resistant prostate cancer subline.
In vitro cellular & developmental biology. Animal 1997;33(3):147-9.
1997: Verma R S; Batish S D; Gogineni S K; Kleyman S M; Stetka D G
Centromeric alphoid DNA heteromorphisms of chromosome 21 revealed by FISH-technique.
Clinical genetics 1997;51(2):91-3.
1997: Kleyman S M; Parekh A J; Rodriguez A R; Conte R A; Verma R S
Paracentric inversion involving the long arm of chromosome 9 resulting in deletion of abl gene.
American journal of medical genetics 1997;68(4):409-11.
1997: Tarzami S T; Kringstein A M; Conte R A; Verma R S
Unique genomic sequences in human chromosome 16p are conserved in the great apes.
Molecular & general genetics : MGG 1997;253(4):512-4.
1997: Verma R S; Kleyman S M; Conte R A
An unusual G-negative band within 1qh region a rare variant or an abnormality?
Annales de génétique 1997;40(4):229-31.
1997: Verma R S; Kleyman S M; Conte R A; Laqui-Pili C; Bennett H
Tandem duplication of chromosome 14 (q12q13).
Annales de génétique 1997;40(4):209-10.
1997: Samonte R V; Ramesh K H; Verma R S
Comparative mapping of human alphoid satellite DNA repeat sequences in the great apes.
Genetica 1997;101(2):97-104.
1997: Conte R A; Kleyman S M; Laundon C; Verma R S
Characterization of two extreme variants involving the short arm of chromosome 22: are they identical?
Annales de génétique 1997;40(3):145-9.
1997: Kohn B; Kleyman S M; Conte R A; Macera M J; Glassberg K; Verma R S
Characterization of an isodicentric Y-chromosome for the long arm in a newborn with mixed gonadal dysgenesis.
Annales de génétique 1997;40(1):10-3.
1996: Samonte R V; Conte R A; Ramesh K H; Verma R S
Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9.
Human genetics 1996;98(5):576-80.
1996: Tarzami S T; Kringstein A M; Conte R A; Verma R S
A unique genomic sequence in the Wolf-Hirschhorn syndrome [WHS] region of humans is conserved in the great apes.
Genetica 1996;98(2):217-9.
1996: Ramesh K H; Gupta S; Verma R S
Assignment of human MYCN proto-oncogene to chromosome band 12q24 in higher primates.
Gene 1996;177(1-2):169-72.
1996: Verma R S; Kleyman S M; Azar G M; Conte R A
To rule out chromosomal abnormalities: a sagacious view.
Lancet 1996;348(9035):1173-4.
1996: Verma R S; Kleyman S M; Conte R A
Molecular characterization of an unusual variant of the short arm of chromosome 15 by FISH-technique.
The Japanese journal of human genetics 1996;41(3):307-11.
1996: Gudi R; Elizalde A; Gogineni S K; Macera M J; Badillo A; Verma R S
Characterization of a complex translocation [t(4;9;22)(p16;q34;q11)] in chronic myelogenous leukemia by fluorescence in situ hybridization technique.
Cancer genetics and cytogenetics 1996;90(2):142-5.
1996: Conte R A; Mathews T; Kleyman S M; Verma R S
Molecular characterization of 21p- variant chromosome.
Clinical genetics 1996;50(2):103-5.
1996: Verma R S; Ramesh K H; Samonte R V; Conte R A
Mapping the homolog of the human Rb1 gene to chromosome 14 of higher primates.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(8):591-2.
1996: Samonte R V; Ramesh K H; Verma R S
Regional localization of human M-BCR gene to chromosome 23 band q11 in the great apes.
Genetica 1996;98(1):111-3.
1996: Verma R S; Kleyman S M; Giridharan R; Ramesh K H
A de novo interstitial deletion of chromosome 15 band q25 as revealed by FISH-technique.
Clinical genetics 1996;49(6):303-5.
1996: Samonte R V; Conte R A; Verma R S
Conservation of p58 and c-myc protooncogene sequences in the great apes.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1996;4(4):321-2.
1996: Gogineni S K; da Costa M; Verma R S
A new translocation, t(5;21)(q13;q22) in acute myelogenous leukemia.
Cancer genetics and cytogenetics 1996;88(2):167-9.
1996: Ramesh K H; Verma R S
Breakpoints in alpha, beta, and satellite III DNA sequences of chromosome 9 result in a variety of pericentric inversions.
Journal of medical genetics 1996;33(5):395-8.
1996: Macera M J; Hyde P; Peddanna N; Szabo P; Gogineni S K; Verma R S
T-cell receptor J beta 1/J beta 2 locus rearrangements in an HTLV-1-positive T-cell lymphoma with complex chromosomal aberrations.
American journal of hematology 1996;52(1):53-7.
1996: Verma R S; Gogineni S K; Kleyman S M; Mann D N
Retrieval of aneuploidy by FISH-technique in a case with 46,XX/47,XXX/47,XX,+8.
The Japanese journal of human genetics 1996;41(1):215-9.
1996: Conte R A; Kleyman S M; Klein V; Bialer M G; Verma R S
Characterization of a de novo t(Y;9) (q11.2;q22) by FISH technique.
Annales de génétique 1996;39(1):10-5.
1996: Verma R S; Ramesh K H; Mathews T; Kleyman S M; Conte R A
Centromeric alphoid sequences are breakage prone resulting in pericentromeric inversion heteromorphism of qh region of chromosome 1.
Annales de génétique 1996;39(4):205-8.
1996: Ramesh K H; Shah H O; Sherman J; Lin J H; Verma R S
Characterization of a derivative chromosome 17 by fish-technique.
Annales de génétique 1996;39(3):177-80.
1996: Ramesh K H; Verma R S
Parental origin of the extra chromosome 18 in Edwards syndrome.
Annales de génétique 1996;39(2):110-2.
1995: Conte R A; Luke S; Verma R S
Characterization of a ring chromosome 21 by FISH-technique.
Clinical genetics 1995;48(4):188-91.
1995: Peddanna N; Holt S; Verma R S
Genetics of gastric cancer.
Anticancer research 1995;15(5B):2055-64.
1995: Luke S; Gandhi S; Verma R S
Conservation of the Down syndrome critical region in humans and great apes.
Gene 1995;161(2):283-5.
1995: Gogineni S K; Elizaide A; Sanchez M A; Verma R S
Characterization of 7q--by FISH technique of a case with acute myelogenous leukemia evolving from agnogenic myeloid metaplasia.
Leukemia research 1995;19(7):481-3.
1995: Conte R A; Pitter J H; Verma R S
Molecular characterization of trisomic segment 3p24.1-->3pter: a case with review of the literature.
Clinical genetics 1995;48(1):49-53.
1995: Luke S; Verma R S
Human (Homo sapiens) and chimpanzee (Pan troglodytes) share similar ancestral centromeric alpha satellite DNA sequences but other fractions of heterochromatin differ considerably.
American journal of physical anthropology 1995;96(1):63-71.
1995: Verma R S; Batish S D; Ramesh K H; Gogineni S K
Are we FISHing in troubled waters?
Cellular & molecular biology research 1995;41(2):81-4.
1995: Macera M J; Verma R S; Conte R A; Bialer M G; Klein V R
Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9.
Cytogenetics and cell genetics 1995;69(3-4):235-9.
1994: Conte R A; Verma R S
Counterstained enhancement of TaqI resistant sites after distamycin A/diamidinophenylindole treatment.
Histochemistry 1994;102(6):433-5.
1994: Macera M J; Sherman J; Shah H O; Blumberg D L; Buttice L S; Lin J H; Verma R S
Identification of a non-fluorescent isodicentric Y chromosome by molecular cytogenetic techniques.
Clinical genetics 1994;46(5):364-7.
1994: Luke S; Verma R S; Giridharan R; Conte R A; Macera M J
Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome.
American journal of medical genetics 1994;51(3):232-3.
1994: Verma R S; Luke S
Evolutionary divergence of human chromosome 9 as revealed by the position of the ABL protooncogene in higher primates.
Molecular & general genetics : MGG 1994;243(4):369-73.
1994: Macera M J; DiPillo F; Szabo P; Ramirez R; Gogineni S; Verma R S
T-cell receptor J beta I/J beta II locus rearrangements concurring with a complex chromosomal aberration in an HTLV-1 positive T-cell lymphoma.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1994;8(3):420-4.
1994: Luke S; Aggarwal G; Stetka D G; Verma R S
Alphoid DNA diversity of a so-called monocentric Robertsonian fusion.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1994;2(1):73-5.
1994: Macera M J; Sanchez M A; Elizalde A M; Gogineni S K; Verma R S
New translocations [t(6;15)(p25;q22) and t(6;19)(q16;q13.3)] with t(9;22)(q34;q11) in a Ph-positive chronic myelogenous leukemia.
Cancer genetics and cytogenetics 1994;72(1):65-7.
1994: Verma R S; Conte R A; Mathews T; Luke S
Monozygotic twinning in a female with triple X[47,XXX].
Gynecologic and obstetric investigation 1994;37(4):279-80.
1994: Mathews T; Agarwal A K; Verma R S
In situ nick translation of human chromosomes with the restriction endonuclease Pvu II [5' CAG decreases CTG 3']
Cytobios 1994;78(315):249-53.
1994: Christodoulidou F; Silver R T; Macera M J; Verma R S
Unusual clonal evolution during blast crisis of chronic myeloid leukaemia (CML)
European journal of cancer (Oxford, England : 1990) 1994;30A(7):1040-1.
1994: Verma R S; Luke S; Conte R A
FISH technique. What's all the fuss about?
Genetic analysis, techniques and applications 1994;11(4):106-9.
1994: Luke S; Birnbaum R; Verma R S
Centromeric and telomeric repeats are stable in nonagenarians as revealed by the double hybridization fluorescent in situ technique.
Genetic analysis, techniques and applications 1994;11(3):77-80.
1993: Luke S; Verma R S
The genomic synteny at DNA level between human and chimpanzee chromosomes.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1993;1(4):215-9.
1993: Macera M J; Szabo P; Lin J H; DeSalvo A T; Shah H O; Verma R S
Direct visualization of the transposed ABL gene in a duplicated masked Ph chromosome.
Genes, chromosomes & cancer 1993;8(2):127-30.
1993: Verma R S; Luke S; Brennan J P; Mathews T; Conte R A; Macera M J
Molecular topography of the secondary constriction region (qh) of human chromosome 9 with an unusual euchromatic band.
American journal of human genetics 1993;52(5):981-6.
1993: Navsaria D; Mathews T; Conte R A; Verma R S
Chromosomal anomalies in 1,000 children referred with suspected genetic disorders.
Human heredity 1993;43(3):137-40.
1993: Verma R S; Conte R A; Macera M J; Khan A S; Hebi S; Masoud A A; al Zaman A; al Bader M
Molecular characterization of a complex translocation in a newborn infant.
American journal of medical genetics 1993;46(1):104-8.
1993: Verma R S; da Costa M; Gogineni S K; Palermo G
New translocation involving homologous chromosome 3 in acute myelogenous leukemia (M2)
American journal of hematology 1993;42(4):398-9.
1993: Luke S; Verma R S
Telomeric repeat [TTAGGG]n sequences of human chromosomes are conserved in chimpanzee (Pan troglodytes).
Molecular & general genetics : MGG 1993;237(3):460-2.
1992: Luke S; Verma R S; Conte R A; Mathews T
Molecular characterization of the secondary constriction region (qh) of human chromosome 9 with pericentric inversion.
Journal of cell science 1992;103 ( Pt 4)():919-23.
1992: Christodoulidou F; Silver R T; Macera M J; Verma R S
Disappearance of a highly unusual clone, 46,XY,del(7)(p12),t(9;22)(q34;q11) in chronic myeloid leukemia after treatment with recombinant interferon and cytosine arabinoside.
Cancer genetics and cytogenetics 1992;64(2):174-7.
1992: Verma R S; Conte R A; Luke S; Sindwani V; Macera M J
Deciphering the fluorescent variability of human genomic heterochromatin by DA/DAPI technique.
Clinical genetics 1992;42(5):267-70.
1992: Verma R S; Luke S; Mathews T; Conte R A
Molecular characterization of the smallest secondary constriction region (qh) of human chromosome 16.
Genetic analysis, techniques and applications 1992;9(5-6):140-2.
1992: Verma R S; Luke S
Variations in alphoid DNA sequences escape detection of aneuploidy at interphase by FISH technique.
Genomics 1992;14(1):113-6.
1992: Macera M J; Szabo P; Verma R S
Chromosomal localization of HTLV-1 viral integration sites using in situ hybridization: detection of a novel IL2R fragment.
Molecular & general genetics : MGG 1992;234(3):466-74.
1992: Ramirez W R; Rosenthal C J; Gogineni S K; Verma R S
Trisomy 8 and 11 in refractory anemia with excess blasts in transformation (RAEB-T).
Cancer genetics and cytogenetics 1992;62(1):98-9.
1992: Luke S; Verma R S
Detection of the heteromorphic spectrum of heterochromatin in the human genome by in situ digestion using restriction endonuclease AluI.
American journal of medical genetics 1992;43(6):1026-9.
1992: Conte R A; Luke S; Verma R S
Molecular characterization of "inverted" pericentromeric heterochromatin of chromosome 3.
Histochemistry 1992;97(6):509-10.
1992: Macera M J; Szabo P; Wadgaonkar R; Siddiqui M A; Verma R S
Localization of the gene coding for ventricular myosin regulatory light chain (MYL2) to human chromosome 12q23-q24.3.
Genomics 1992;13(3):829-31.
1992: Verma R S; Conte R A; Pitter J H
Tandem duplication of the terminal band of the long arm of chromosome 7 (dir dup (7)(q36----qter)).
Journal of medical genetics 1992;29(5):344-5.
1992: Verma R S; Conte R A; Sayegh S E; Kanjilal D
The interstitial deletion of bands q33-35 of long arm of chromosome 7: a review with a new case report.
Clinical genetics 1992;41(2):82-6.
1992: Verma R S; Conte R A; Pitter J H; Luke S
Pericentric inversion of chromosome 7 (inv(7) (p22q11.2)) and ring chromosome 8 (r(8) (p23q24.3)) in a girl with minor anomalies.
Journal of medical genetics 1992;29(1):66-7.
1992: Luke S; Bennett H S; Pitter J H; Verma R S
A new case of monosomy for 17q25----qter due to a maternal translocation [t(3;17)(p12;q24)]
Annales de génétique 1992;35(1):48-50.
1992: Conte R A; Sayegh S E; Verma R S
An apparent balanced translocation [t(9;11)(p21.2;p14.2)] in a neonate with dysmorphic features.
Annales de génétique 1992;35(3):164-5.
1992: Luke S; Mathews T; Verma R S
Evolution of pericentromeric heterochromatin of human X chromosome.
Genetica 1992;87(1):63-4.
1992: Mathews T; Navsaria D; Verma R S
Prenatal cytogenetic diagnosis of 1,400 consecutive amniocenteses.
Gynecologic and obstetric investigation 1992;34(2):122-3.
1992: Rao P H; Cesarman G; Coleman M; Acaron S; Verma R S
Cytogenetic evidence for extramedullary blast crisis with t(8;13)(q11;p11) in chronic myelomonocytic leukemia.
Acta haematologica 1992;88(4):201-3.
1991: Verma R S; Macera M J; da Costa M; Bradley T; Christodoulidou F
del(2)(p23): a consistent recurrent abnormality in acute myelogenous leukemia.
Cancer genetics and cytogenetics 1991;57(2):175-9.
1991: Mathews T; Verma R S
Enhancement of amniotic fluid cell growth for genetic amniocentesis.
Clinical genetics 1991;40(3):190-3.
1991: Verma R S; Luke S
Heteromorphisms of pericentromeric heterochromatin of chromosome 19.
Genetic analysis, techniques and applications 1991;8(6):179-80.
1991: Grossman A; Silver R T; Szatroswki T P; Gutfriend A; Verma R S; Benn P A
Densitometric analysis of Southern blot autoradiographs and its application to monitoring patients with chronic myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(7):540-7.
1991: Christodoulidou F; Coleman M; Macera M J; Verma R S
Complex chromosomal abnormalities in a patient with refractory anemia with excess blasts (RAEB).
Cancer genetics and cytogenetics 1991;54(2):229-32.
1991: Verma R S; Luke S; Conte R A; Macera M J
A so-called rare heteromorphism of the human genome.
Cytogenetics and cell genetics 1991;56(1):63.
1990: Silver R T; Benn P; Verma R S; Coleman M; Soper L; Gutfriend A
Recombinant gamma-interferon has activity in chronic myeloid leukemia.
American journal of clinical oncology 1990;13(1):49-54.
1989: Verma R S; Macera M J; Benn P; Groffen J
Molecular characterization of variant translocations in chronic myelogenous leukemia.
Oncogene 1989;4(9):1145-8.
1989: Ramirez G M; Macera M J; Verma R S
Two new chromosomal abnormalities in chronic myelogenous leukemia 46,XY,t(9;15;22)(q34;q22;q11) and 46,XY,t(6;9;12;22)(p21;q34;q24;q11).
Cancer genetics and cytogenetics 1989;38(1):115-9.
1989: Macera M J; Babu A; Verma R S
Application of DA/DAPI technique in cancer cytogenetics.
Oncology 1989;46(1):61-2.
1989: Macera M J; Szabo P; Verma R S
A simple method for short-term culturing bone marrow and unstimulated blood from acute leukemias.
Leukemia research 1989;13(9):729-34.
1988: Macera M J; Botti A C; Verma R S; Coleman M; Thomas E D
Clonal expansion after bone marrow transplantation in a patient with chronic myelogenous leukemia.
Blut 1988;57(5):303-6.
1988: Weinstein M E; Grossman A; Perle M A; Wilmot P L; Verma R S; Silver R T; Arlin Z; Allen S L; Amorosi E; Waintraub S E
The karyotype of Philadelphia chromosome-negative, bcr rearrangement-positive chronic myeloid leukemia.
Cancer genetics and cytogenetics 1988;35(2):223-9.
1988: Botti A C; Silver R T; Macera M J; Benn P; Verma R S
A new translocation involving chromosomes 8 and 9 in a Philadelphia-negative chronic myelogenous leukemia.
Cancer genetics and cytogenetics 1988;35(1):51-4.
1988: Verma R S; Thomas S; Coleman M; Silver R T
Spatial relationship of chromosomes 9 and 22 at metaphase in patients with chronic myelogenous leukemia (CML).
International journal of cancer. Journal international du cancer 1988;41(6):829-31.
1988: Botti A C; Diamond G R; Verma R S
Lymphoma and acquired immunodeficiency syndrome: cytogenetic and molecular correlates.
European journal of cancer & clinical oncology 1988;24(5):939-41.
1988: Verma R S; Macera M J; Babu A
The role of heterochromatin in the origin of isochromosome 1 in neoplastic cells.
European journal of cancer & clinical oncology 1988;24(5):821-3.
1988: Verma R S; Macera M J; Silver R T; Coleman M
Origin of near-haploidy in malignant hematopoietic cells.
Leukemia research 1988;12(11-12):941-50.
1987: Powell D R; Verma R S
Hypo- and hyperdiploidy in cultured amniocytes.
In vivo (Athens, Greece) 1987;1(4):235-6.
1987: Verma R S; Macera M J
Genomic diversity of Philadelphia-positive chronic myelogenous leukemia.
Leukemia research 1987;11(9):833-42.

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